7645589

Source:http://linkedlifedata.com/resource/pubmed/id/7645589

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0016395, umls-concept:C0017337, umls-concept:C0039082, umls-concept:C0043297, umls-concept:C0443299, umls-concept:C0449774, umls-concept:C0678227, umls-concept:C0796070, umls-concept:C1417193, umls-concept:C1551338
pubmed:issue	1
pubmed:dateCreated	1995-9-21
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/7645589-8116674, http://linkedlifedata.com/resource/pubmed/commentcorrection/7645589-8267001
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7708900
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	May
pubmed:issn	0148-7299
pubmed:author	pubmed-author:HappleRR, pubmed-author:MückeJJ, pubmed-author:TheileHH
pubmed:issnType	Print
pubmed:day	22
pubmed:volume	57
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	117-8
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:7645589-Adult, pubmed-meshheading:7645589-Child, Preschool, pubmed-meshheading:7645589-Corneal Diseases, pubmed-meshheading:7645589-Eye Abnormalities, pubmed-meshheading:7645589-Female, pubmed-meshheading:7645589-Focal Dermal Hypoplasia, pubmed-meshheading:7645589-Humans, pubmed-meshheading:7645589-Skin Abnormalities, pubmed-meshheading:7645589-Skin Diseases, pubmed-meshheading:7645589-Syndrome, pubmed-meshheading:7645589-X Chromosome
pubmed:year	1995
pubmed:articleTitle	MIDAS syndrome respectively MLS syndrome: a separate entity rather than a particular lyonization pattern of the gene causing Goltz syndrome.
pubmed:publicationType	Letter, Comment, Case Reports